NM_000071.3(CBS):c.34C>T (p.Pro12Ser) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 21, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000197083.10
Allele description [Variation Report for NM_000071.3(CBS):c.34C>T (p.Pro12Ser)]
NM_000071.3(CBS):c.34C>T (p.Pro12Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens kinesin light chain 1 (KLC1), transcript variant 1, mRNA
Homo sapiens kinesin light chain 1 (KLC1), transcript variant 1, mRNAgi|1890267732|ref|NM_005552.5|Nucleotide
-
Mus musculus chromosome X, clone CT7-41M10
Mus musculus chromosome X, clone CT7-41M10gi|7594633|emb|AL136328.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 16, 2024